Rosemarie Smith

3.7k total citations
21 papers, 744 citations indexed

About

Rosemarie Smith is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Rosemarie Smith has authored 21 papers receiving a total of 744 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 8 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Rosemarie Smith's work include Congenital Anomalies and Fetal Surgery (3 papers), Prenatal Screening and Diagnostics (3 papers) and Pediatric Hepatobiliary Diseases and Treatments (3 papers). Rosemarie Smith is often cited by papers focused on Congenital Anomalies and Fetal Surgery (3 papers), Prenatal Screening and Diagnostics (3 papers) and Pediatric Hepatobiliary Diseases and Treatments (3 papers). Rosemarie Smith collaborates with scholars based in United States, Germany and Canada. Rosemarie Smith's co-authors include Ian D. Krantz, Nancy B. Spinner, Elizabeth Goldmuntz, Angela E. Lin, Elaine H. Zackai, David A. Piccoli, Heather J. Stalker, Michele Clemens, Amy E. Roberts and Roberto T. Zori and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Rosemarie Smith

18 papers receiving 729 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rosemarie Smith United States 11 409 336 151 105 92 21 744
Angus Dobbie United Kingdom 12 402 1.0× 284 0.8× 108 0.7× 57 0.5× 35 0.4× 20 675
Patrizia Ronchetto Italy 11 344 0.8× 297 0.9× 347 2.3× 133 1.3× 40 0.4× 28 841
Thomas A. Maher United States 13 270 0.7× 147 0.4× 112 0.7× 137 1.3× 26 0.3× 23 586
Marcello Niceta Italy 18 489 1.2× 304 0.9× 60 0.4× 45 0.4× 43 0.5× 53 810
Marie-Laure Kottler France 15 456 1.1× 406 1.2× 86 0.6× 26 0.2× 75 0.8× 23 981
Flavio Faletra Italy 15 251 0.6× 267 0.8× 59 0.4× 40 0.4× 25 0.3× 84 649
Oana Caluseriu Canada 14 583 1.4× 389 1.2× 116 0.8× 138 1.3× 208 2.3× 37 876
Pagon Ra United States 6 450 1.1× 260 0.8× 55 0.4× 38 0.4× 49 0.5× 291 791
Gülen Eda Ütine Türkiye 14 367 0.9× 373 1.1× 66 0.4× 71 0.7× 45 0.5× 114 715
Ivana Matera Italy 16 290 0.7× 192 0.6× 281 1.9× 145 1.4× 34 0.4× 26 804

Countries citing papers authored by Rosemarie Smith

Since Specialization
Citations

This map shows the geographic impact of Rosemarie Smith's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rosemarie Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rosemarie Smith more than expected).

Fields of papers citing papers by Rosemarie Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosemarie Smith. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rosemarie Smith. The network helps show where Rosemarie Smith may publish in the future.

Co-authorship network of co-authors of Rosemarie Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Rosemarie Smith. A scholar is included among the top collaborators of Rosemarie Smith based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rosemarie Smith. Rosemarie Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
McDonald‐McGinn, Donna M., T. Blaine Crowley, Daniel E. McGinn, et al.. (2024). P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome. SHILAP Revista de lepidopterología. 2. 101114–101114.
2.
Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations
3.
Dyment, David A., Pauline Terhal, Cecilie F. Rustad, et al.. (2019). De novo substitutions of TRPM3 cause intellectual disability and epilepsy. European Journal of Human Genetics. 27(10). 1611–1618. 44 indexed citations
4.
Levin, Mark, Sulagna C. Saitta, Karen W. Gripp, et al.. (2018). Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients. American Journal of Medical Genetics Part A. 176(8). 1711–1722. 22 indexed citations
5.
Andersen, Erica, Erin E. Baldwin, Sara Ellingwood, Rosemarie Smith, & Allen N. Lamb. (2014). Xq28 duplication overlapping the int22h‐1/int22h‐2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability. American Journal of Medical Genetics Part A. 164(7). 1795–1801. 31 indexed citations
6.
Wax, Joseph R., et al.. (2011). Stepwise sequential aneuploidy screening in clinical practice. Journal of Clinical Ultrasound. 40(1). 26–30.
7.
Bachmann‐Gagescu, Ruxandra, Heather C. Mefford, Charles A. Cowan, et al.. (2010). Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Genetics in Medicine. 12(10). 641–647. 137 indexed citations
8.
Bauer, Robert C., Rosemarie Smith, Jennifer Gerfen, et al.. (2010). Jagged1 (JAG1) mutations in patients with tetralogy of fallot or pulmonic stenosis. Human Mutation. 31(5). 594–601. 84 indexed citations
9.
Wax, Joseph R., et al.. (2010). Prenatal Sonographic Findings in Human Disorganization Syndrome. Journal of Ultrasound in Medicine. 29(2). 301–305.
10.
Milunsky, Jeff M., Tom A. Maher, Geping Zhao, et al.. (2009). TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome. The American Journal of Human Genetics. 84(2). 301–301. 7 indexed citations
11.
Moeschler, John B., Roberto Amato, Leah W. Burke, et al.. (2009). Improving genetic health care: A Northern New England pilot project addressing the genetic evaluation of the child with developmental delays or intellectual disability. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 241–254. 13 indexed citations
12.
Milunsky, Jeff M., Tom A. Maher, Geping Zhao, et al.. (2008). TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome. The American Journal of Human Genetics. 82(5). 1171–1177. 161 indexed citations
13.
Wax, Joseph R., Michael G. Pinette, Rosemarie Smith, Angelina Cartin, & Jacquelyn Blackstone. (2008). First‐trimester prenatal sonographic diagnosis of omphalocele‐exstrophy‐imperforate anus‐spinal defects complex. Journal of Clinical Ultrasound. 37(3). 171–174. 8 indexed citations
14.
Raile, Klemens, Jürgen Klammt, Annika Keller, et al.. (2006). Clinical and Functional Characteristics of the Human Arg59Ter Insulin-Like Growth Factor I Receptor (IGF1R) Mutation: Implications for a Gene Dosage Effect of the Human IGF1R. The Journal of Clinical Endocrinology & Metabolism. 91(6). 2264–2271. 61 indexed citations
15.
Wheeler, Patricia G., Rosemarie Smith, Henry L. Dorkin, et al.. (2001). Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical center. Genetics in Medicine. 3(6). 411–415. 35 indexed citations
16.
Smith, Rosemarie, et al.. (2001). Grebe syndrome in Vietnamese sisters: not Agent Orange. Clinical Genetics. 59(1). 25–27. 1 indexed citations
17.
Krantz, Ian D., Rosemarie Smith, Elaine H. Zackai, et al.. (1999). Jagged1 mutations in patients ascertained with isolated congenital heart defects. American Journal of Medical Genetics. 84(1). 56–60. 111 indexed citations
18.
Krantz, Ian D., Rosemarie Smith, Elaine H. Zackai, et al.. (1999). Jagged1 mutations in patients ascertained with isolated congenital heart defects. American Journal of Medical Genetics. 84(1). 56–60. 6 indexed citations
19.
Smith, Rosemarie, et al.. (1989). Building-Based Instructional Improvement: the Principal as an Instructional Leader. NASSP Bulletin. 73(518). 10–16. 3 indexed citations
20.
Thakker, Rajesh V., Melanie J. Davies, K E Davies, et al.. (1986). LOCALIZATION OF THE GENE CAUSING X-LINKED HYPOPHOSPHATEMIC RICKETS. QJM. 61. 1071–1072. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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